Regional Study Coordinator at Labcorp

Suzhou City, Jiangsu, China -

Full Time

Start Date

Immediate

Expiry Date

23 Mar, 26

Salary

0.0

Posted On

23 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Communication, Organizational Skills, Attention To Detail, Teamwork, Customer Service, Process Improvement, Logistics Management, Monitoring, Performance Metrics, Interpersonal Skills, Negotiation Skills, Microsoft Word, Excel, MS Access, Outlook

Industry

Medical Practices

Description

Job Summary: The Regional Study Coordinator (RSC) is responsible for the successful delivery of alloperations of a clinical study in their specific area of the world. The RSC acts as theappointed Liaison between Global Project Management, Client Representatives and other CCLS departments involved in the clinical study to ensure the successful management of regional study responsibilities. The Regional Study Coordinator may communication with the Client when a task is being delegated by the Global Study Manager. Regular communication is essential with the appointed Global Study Manager who is accountable for the entire protocol. This position must be in compliance with the CCLS Global Project Management strategy and deliver outstanding customer satisfaction and performance. Essential Job Duties: 1. Act as regional liaison between Global Study Manager and various CCLS departments involved in the study 2. Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors)and the corresponding local CCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact 3. Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure 4. Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead 5. Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial 6. Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development 7. Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop 8. Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed. 9. Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan 10. Demonstrate ability to work in a matrix environment where task assignments can be channeled down to be completed by Regional Study Coordinators while other task assignments will need to be delegated to other functional groups; demonstrate flexibility in handling both categories of tasks 11. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date 12. Comply with CCLS Global Project Management strategy 13. Support a culture of continuous improvement, quality and productivity 14. Other duties as assigned The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above Experience: Minimum Required: Demonstrated ability to plan and prioritize. Demonstrated communication and organizational skills. Demonstrated attention to detail. Proven ability to excel in a fast paced environment Proven teamwork Proven experience and knowledge of processes and tools used in department Demonstrated ability to liaise with internal departments Demonstrated ability to facilitate meetings Demonstrated participation in process improvement initiatives 2 years customer service experience, preferable in pharmaceutical industry (Education may be substituted for experience) Education/Qualifications/Certifications and Licenses: Ability to use computer and office software applications (e.g. Microsoft Word, Excel, MSAccess and Outlook) Strong interpersonal skills Strong in English Influence and negotiation skills Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.

Responsibilities

The Regional Study Coordinator is responsible for managing all operations of a clinical study in their region, acting as a liaison between various departments and client representatives. They ensure compliance with project management strategies and maintain regular communication with the Global Study Manager.